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Novel KCNV2 mutations in cone dystrophy with supernormal rod electroretinogram.
Am J Ophthalmol. 2008 Jun;145(6):1099-106. doi: 10.1016/j.ajo.2008.02.004. Epub 2008 Apr 9.
Am J Ophthalmol. 2008.
PMID: 18400204
[Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].
Hamel CP, Griffoin JM, Bazalgette C, Lasquellec L, Duval PA, Bareil C, Beaufrère L, Bonnet S, Eliaou C, Marlhens F, Schmitt-Bernard CF, Tuffery S, Claustres M, Arnaud B.
Hamel CP, et al.
J Fr Ophtalmol. 2000 Dec;23(10):985-95.
J Fr Ophtalmol. 2000.
PMID: 11139690
French.
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Mutations in RPE65 cause Leber's congenital amaurosis.
Marlhens F, Bareil C, Griffoin JM, Zrenner E, Amalric P, Eliaou C, Liu SY, Harris E, Redmond TM, Arnaud B, Claustres M, Hamel CP.
Marlhens F, et al.
Nat Genet. 1997 Oct;17(2):139-41. doi: 10.1038/ng1097-139.
Nat Genet. 1997.
PMID: 9326927
No abstract available.
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Accuracy of PlusOptix A09 distance refraction in pediatric myopia and hyperopia.
Payerols A, Eliaou C, Trezeguet V, Villain M, Daien V.
Payerols A, et al.
BMC Ophthalmol. 2016 Jun 1;16:72. doi: 10.1186/s12886-016-0247-8.
BMC Ophthalmol. 2016.
PMID: 27246869
Free PMC article.
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[Cavitary choroidal melanoma in a child].
Faraj H, Levy-Gabriel C, Lumbroso-Le Rouic L, Chefchaouni MC, Langmann ME, Orbach D, Sastre X, Couturier J, Eliaou CM, Desjardins L.
Faraj H, et al. Among authors: eliaou cm.
J Fr Ophtalmol. 2006 May;29(5):559-63. doi: 10.1016/s0181-5512(06)73811-6.
J Fr Ophtalmol. 2006.
PMID: 16885832
French.
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